intErnet-based iNterventions FOR Cardiac arrEst suRvivors

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

137 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-08-05

Study Completion Date

2026-10-01

Brief Summary

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Anxiety, depression and cognitive impairment symptoms are common among cardiac arrest survivors. This randomized clinical trial will test whether an internet-based lifestyle intervention administered through a web app can foster anxiety and depression symptoms in patients who survived an out-of-hospital cardiac arrest and suffer from these symptoms

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Detailed Description

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Conditions

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Cognitive Impairment Depression, Anxiety Cardiac Arrest Quality of Life Social Functioning Sexual Dysfunction

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Outcome Assessors

The assessor will be unaware about the study arm allocation of the patient

Study Groups

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Lifestyle intervention

Group Type EXPERIMENTAL

Lifestyle intervention

Intervention Type BEHAVIORAL

Multimodal web-based intervention programme on anxiety, depression and cognitive impairment consisting of knowledge development sessions and practical/gaming sessions focused on different domains: cognitive competence, socio-relational competence and emotions/affectivity, and physical activity-nutrition

Control

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Lifestyle intervention

Multimodal web-based intervention programme on anxiety, depression and cognitive impairment consisting of knowledge development sessions and practical/gaming sessions focused on different domains: cognitive competence, socio-relational competence and emotions/affectivity, and physical activity-nutrition

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Hospital discharge after out-of-hospital cardiac arrest with Cerebral Performance Category 1 or 2
* HADS anxiety or depression ≥ 8 and/or TICS ≤ 31
* Informed consent for participation in the study
* Native Italian speaker or adequate understanding of the Italian language
* Adequate ability to use the web to guarantee access to the contents